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saypha MagIQ 39507

by Obagi Cosmeceuticals LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00362032907017 UDI-DI Date27 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
saypha MagIQ
Generic Name
Dermal tissue reconstructive material, microbe-derived, anaesthetic
Model / Reference
39507
Primary DI / UDI-DI
00362032907017
FDA Product Code
LMH
GMDN Term
Dermal tissue reconstructive material, microbe-derived, anaesthetic
Device Class
Class III
GUDID distribution status
In Commercial Distribution

Other devices from Obagi Cosmeceuticals LLC

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (6)

  • Contains Latex: No
  • Over-the-Counter: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No